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Items: 1 to 20 of 128

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7074641inversion1nstd229human GRCh38 chr12: 52,659,002-59,632,575 , GRCh37.p13 chr12: 53,052,786-60,026,356 , LOC105369777, 292 more genes
    nsv7071794inversion1nstd229human GRCh38 chr12: 54,130,507-54,130,566 , GRCh37.p13 chr12: 54,524,291-54,524,350 SMUG1, LINC02381
    nsv7069901inversion1nstd229human GRCh38 chr12: 51,176,082-54,825,440 , GRCh37.p13 chr12: 51,569,865-55,219,224 , HOXC5, 158 more genes
    nsv6930650copy number variation1nstd229human GRCh38 chr12: 54,040,740-54,211,543 , GRCh37.p13 chr12: 54,434,524-54,605,327 LOC100240734, LOC102724030, 7 more genes
    nsv6930479copy number variation1nstd229human GRCh38 chr12: 54,107,012-54,133,899 , GRCh37.p13 chr12: 54,500,796-54,527,683 LINC02381, FLJ12825, 1 more genes
    nsv6929428copy number variation1nstd229human GRCh38 chr12: 54,132,594-54,162,991 , GRCh37.p13 chr12: 54,526,378-54,556,775 LOC102724030, LINC02381, 2 more genes
    nsv6918266copy number variation1nstd229human GRCh38 chr12: 54,133,031-54,135,952 , GRCh37.p13 chr12: 54,526,815-54,529,736 LINC02381, SMUG1
    nsv6143026copy number variation1nstd206human GRCh38 chr12: 48,500,915-111,724,058 , GRCh37.p13 chr12: 48,894,698-112,161,862 , LINC00592, 1206 more genes
    nsv6132426copy number variation1nstd213human GRCh37 chr12: 52,740,000-55,260,001 , GRCh38.p12 chr12: 52,346,216-54,866,217 , HOXC4, 122 more genes
    nsv5652850insertion1nstd207human GRCh38 chr12: 54,129,490-54,129,490 , GRCh37.p13 chr12: 54,523,274-54,523,274 LINC02381, SMUG1
    nsv5137452mobile element insertion1nstd203human GRCh38 chr12: 54,125,427-54,125,440 , GRCh37.p13 chr12: 54,519,211-54,519,224 SMUG1, LINC02381
    nsv5040224inversion1nstd200human GRCh38 chr12: 47,213,128-71,357,206 , GRCh37.p13 chr12: 47,606,911-71,750,986 , NR4A1, 686 more genes
    nsv5036282inversion1nstd200human GRCh38 chr12: 52,338,357-95,425,642 , GRCh37.p13 chr12: 52,732,141-95,819,418 , MIR6502, 769 more genes
    nsv4883504inversion1nstd200human GRCh37 chr12: 52,732,141-95,819,418 , GRCh38.p12 chr12: 52,338,357-95,425,642 , MYL6B, 769 more genes
    nsv4755205inversion1nstd199human GRCh37 chr12: 25,956,127-125,801,151 , GRCh38.p12 chr12: 25,803,193-125,316,605 , ACACB, 1787 more genes
    nsv4736781copy number variation1nstd199human GRCh37 chr12: 25,957,322-125,801,148 , GRCh38.p12 chr12: 25,804,388-125,316,602 , RNA5SP368, 1787 more genes
    nsv4611340copy number variation1nstd183human GRCh37 chr12: 54,469,102-54,519,985 , GRCh38.p12 chr12: 54,075,318-54,126,201 SMUG1, LINC02381, 3 more genes
    nsv4559196inversion1nstd166human GRCh37.p13 chr12: 51,569,865-55,219,228 , GRCh38.p12 chr12: 51,176,082-54,825,444 , EIF4B, 163 more genes
    nsv4436658copy number variation1nstd102humanPathogenic GRCh37 chr12: 53,784,698-54,741,363 , GRCh38.p12 chr12: 53,390,914-54,347,579 , CALCOCO1, 53 more genes
    nsv4425829copy number variation1nstd174human GRCh37 chr12: 54,467,303-54,528,384 , GRCh38.p12 chr12: 54,073,519-54,134,600 SMUG1, FLJ12825, 3 more genes
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